LITHIUM CARBONATE ER
Generic: LITHIUM CARBONATE
Glenmark Pharmaceuticals Inc.Manufacturer
ORALRoute
LITHIUM CARBONATEActive Substance
2011-02-14Original Approval
LITHIUM CARBONATE ER is FDA application ANDA091616, sponsored by GLENMARK PHARMS LTD. Any recalls listed below come from FDA drug enforcement reports, and reaction counts are the number of FAERS adverse event reports that mention the drug and that reaction; a report does not prove the drug caused it.
Top Reported Reactions
1
TOXICITY TO VARIOUS AGENTS
1,217 reports
2
DRUG INEFFECTIVE
1,117 reports
3
TREMOR
1,064 reports
4
DRUG INTERACTION
993 reports
5
NAUSEA
806 reports
6
WEIGHT INCREASED
794 reports
7
INSOMNIA
700 reports
8
DEPRESSION
696 reports
9
FATIGUE
674 reports
10
VOMITING
663 reports